Makale
Tam Makale
Uluslararası
2016
Idiopathic Thrombocytopenic Purpura as Initial Manifestation of Systemic Lupus Erythematosus: A Case Report
TURK OSTEOPOROZ DERGISI-TURKISH JOURNAL OF OSTEOPOROSIS
Cilt 22 · Sayı 2 · ss. 110–112 · 01.08.2016
Özet
Systemic lupus erythematosus (SLE) is a chronic autoimmune disease that can affect almost any organ system. Its presentation and course are highly variable. The classic presentation of SLE in a woman of childbearing age is fever, arthritis, and malar rash triad. However, patients may present rare types of manifestations such as idiopathic thrombocytopenic purpura.
Atıf için künye
Bagcier, F., & Erdal, A. (2016). Idiopathic Thrombocytopenic Purpura as Initial Manifestation of Systemic Lupus Erythematosus: A Case Report. TURK OSTEOPOROZ DERGISI-TURKISH JOURNAL OF OSTEOPOROSIS, 22(2), 110–112. https://doi.org/10.4274/tod.77045
BibTeX
@article{bagcier2016-226077,
author = {Bagcier, Fatih and Erdal, Akın},
title = {Idiopathic Thrombocytopenic Purpura as Initial Manifestation of Systemic Lupus Erythematosus: A Case Report},
journal = {TURK OSTEOPOROZ DERGISI-TURKISH JOURNAL OF OSTEOPOROSIS},
year = {2016},
volume = {22},
number = {2},
pages = {110--112},
issn = {2146-3816},
doi = {10.4274/tod.77045},
url = {https://akademik.atauni.edu.tr/yayinlar/226077-idiopathic-thrombocytopenic-purpura-as-initial-manifestation-of-systemic-lupus}
}